Familial hemophagocytic lymphohistiocytosis. A differential diagnosis with infection-induced hemophagocytic syndromes;La lymphohistiocytose hemophagocytaire familiale. Une affection a differencier des syndromes hemophagocytaires secondaires

Archives d'Anatomie et de Cytologie Pathologiques

Volumn 45, Issue 4, 1997, Pages 208-213

  Boissy, C ^a   Velin, P ^a   Michiels, J F ^a   Diebold, J ^a   Hofman, P ^a  

^a PASTEUR HOSPITAL   (France)

Author keywords

Child; Congenital; Hemophagocytosis; Lymphohistiocytosis

Indexed keywords

CD30 ANTIGEN; COMPLEMENT COMPONENT C3B RECEPTOR; COMPLEMENT COMPONENT C3D RECEPTOR;

ARTICLE; CASE REPORT; DIFFERENTIAL DIAGNOSIS; FAMILIAL DISEASE; HEMOPHAGOCYTIC SYNDROME; HISTIOCYTOSIS; HISTOPATHOLOGY; HUMAN; INFANT; INFECTION; MALE; TWINS; BIOPSY; BONE MARROW; DIZYGOTIC TWINS; FEMALE; GENETICS; PATHOLOGY;

BIOPSY; BONE MARROW; DIAGNOSIS, DIFFERENTIAL; DISEASES IN TWINS; FEMALE; HISTIOCYTOSIS, NON-LANGERHANS-CELL; HUMANS; INFANT; MALE; TWINS, DIZYGOTIC;

EID: 0031303997     PISSN: 0395501X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (20)